Takeda insomnia drug ad removed after FDA warning
US regulators also criticised Takeda for suggesting that the insomnia treatment was safe for use in children. The FDA said that the safety of effectiveness of the drug
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.